Key result
Atorvastatin-fenofibrate pretreatment lowers lipids in acute lipemia mice, identifying cystatin C as a theranostic biomarker.
Why the study?
Dyslipidemia is a major risk factor for cardiovascular disease and atherosclerosis, but the effects of combined atorvastatin and fenofibrate pretreatment required evaluation in poloxamer 407-induced acute lipemia.
Does pretreatment with atorvastatin, fenofibrate, or both improve lipid profiles and alter cystatin C and lysosomal acid lipase expression in a mouse model of acute lipemia?
Does pretreatment with atorvastatin, fenofibrate, or both improve lipid profiles and alter cystatin C and lysosomal acid lipase expression in a mouse model of acute lipemia?
Pretreatment with atorvastatin and fenofibrate improves lipid profiles and increases liver expression of lysosomal acid lipase in a mouse model of acute lipemia, suggesting cystatin C as a potential theranostic biomarker.
Hypothesis-generating in mouse lipemia model; leaves open whether combined atorvastatin-fenofibrate or cystatin C monitoring merits human trials.
Dyslipidemia is a well-known risk factor for the development of cardiovascular diseases and atherosclerosis. The effects of combined pretreatment with atorvastatin and fenofibrate (Tricor) were studied in a mouse model of acute lipemia induced by a general lipase inhibitor, poloxamer 407 (P-407, 250 mg/kg). This lipemia is characterized by significantly increased serum levels of triglycerides (TG), low-density lipoprotein (LDL) cholesterol, together with decreased concentration of high-density lipoprotein (HDL) cholesterol. Atorvastatin pretreatment had a hypolipidemic effect, decreasing concentrations of LDL cholesterol and increasing HDL cholesterol. Pretreatment of mice with fenofibrate decreased TG level, increasing HDL cholesterol. Combined pretreatment with atorvastatin and fenofibrate decreased TG and total cholesterol. Elevation of the serum cystatin C level was found in control and lipemic mice pretreated with atorvastatin, fenofibrate, or both. Liver expression of lysosomal acid lipase increased in atorvastatin- or/and fenofibrate-pretreated groups of lipemic mice. It was concluded that increased expression of lysosomal acid lipase is related to the removal of lipid droplets from hepatocytes, thus preventing acute lipemia. Lastly, cystatin C may be a “theranostic” biomarker for hypolipidemic drugs.
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Короленко et al. (2024) studied Acute lipemia. Atorvastatin, fenofibrate, or both vs. Control was evaluated on Lipid levels (TG, LDL, HDL, total cholesterol), cystatin C, and lysosomal acid lipase expression. Combined pretreatment with atorvastatin and fenofibrate decreased triglycerides and total cholesterol in a mouse model of acute lipemia, with cystatin C identified as a potential theranostic biomarker.
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